Exam 3: Lecture 10, Toxicokinetics & Toxicodynamics Flashcards

1
Q

Major factors influencing toxicity?

A

route and site of exposure

Duration and frequency of exposure

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2
Q

characterization of potential hazard

A
info about chemical
type of effect
dose required to produce the effect
Exposure
disposition
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3
Q

IV Admin

A

directly into blood

Bolus = <10 sec injection 
infusion = slow constant rate
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4
Q

Extravascular admin

A

oral, buccal, sublingual

subq,rectal,topical

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5
Q

Drugs are ore frequently administered….

A

extravascularly and intended to act systemically rather than locally

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6
Q

If TD after oral/dermal similar to TD with AV admin then…

A

chemical is absorbed readily and rapidly

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7
Q

If TD after dermal route is higher than oral then…

A

likely skin provides an affective barrier to absorption

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8
Q

Bioavailability

A

fraction of extravascularly admin dose that reaches systemic circulation intact

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9
Q

First pass loss

A

after taking drug orally, the loss of the drug as it passes through tissues

essentially first pass effect

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10
Q

Most important PK parameters of any drug developed for extravascular admin is….

A

bioavailability

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11
Q

Most common outcome of biotransformation is…

A

is lose of pharmacological activity

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12
Q

Most important PK parameter?

A

clearance

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13
Q

Compartmental approach

A

views body as composed of a number of Pkically distinct compartments

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14
Q

Noncompartmental Approach

A

estimating PK parameters from plasma drug conc vs time profiles without any assumptions of a specific compartmental model for the body

NCA, typically used in study

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15
Q

Based on ICHS9 what’s important to report in TK studies?

A

Peak plasma/serum levels
AUC
Half life

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16
Q

What should you write about in Pk report?

A

Clearance
Distribution
Half-life

17
Q

Which compound safest based on TI?

A

the one with the largest ration between TD50/Ed50